Have you ever heard of HELLP syndrome?

I’m guessing most of you are shaking your head and perhaps asking ChatGPT for a quick explanation…

I had never heard of it either. I certainly never imagined that it would become part of my story.

HELLP syndrome is a rare, life-threatening complication of pregnancy, affecting fewer than 1% of pregnancies. The severe liver complications are even rarer, making cases like mine exceptionally uncommon.

In March 2026, after an emergency c-section to deliver my son, I developed HELLP syndrome and became critically ill. A tear in my liver caused severe blood loss, which required three blood transfusions, two further operations, and five days in intensive care.

The first days of my son’s life, I spent fighting for my own.

We spent the next two weeks together in hospital with my amazing partner Katherine, and although my recovery continues to this day, I am incredibly grateful to be here watching our son grow. Sadly, not every family gets that chance.

My outcome was only possible because of the skill and dedication of the teams at Darent Valley Hospital and King’s College Hospital. However, the cause and prevention of this condition remains unknown.

On 20th March 2027, Katherine and I will walk 17 miles across London between these two hospitals to represent our journey, and to show our gratitude for everything they have done for us.

We’ll also be raising money for Action on Pre-Eclampsia (APEC), a charity that supports families affected by pre-eclampsia and related conditions, including HELLP syndrome. APEC also works to improve antenatal care through education, support vital clinical research, and raise awareness so that more mothers and babies have the chance of a better outcome.

Any donation, no matter how small, is hugely appreciated. If you’re unable to donate, simply liking and sharing this page can make a real difference.

Thank you for reading our story and for supporting our walk.